HGVS | Genome Assembly |
---|---|
NC_000006.12:g.42722049G>T , CM000668.2:g.42722049G>T | GRCh38 |
NC_000006.11:g.42689787G>T , CM000668.1:g.42689787G>T | GRCh37 |
NC_000006.10:g.42797765G>T | NCBI36 |
NG_009176.1:g.5572C>A | |
NG_009176.2:g.5572C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000230381.7:c.286C>A MANE Select | ENSP00000230381.5:p.Pro96Thr | |
ENST00000230381.6:c.286C>A | ENSP00000230381.5:p.Pro96Thr | |
NM_000322.4:c.286C>A | NP_000313.2:p.Pro96Thr | |
XR_427834.2:n.941C>A | ||
XR_926295.1:n.941C>A | ||
XR_427834.4:n.991C>A | ||
XR_926295.3:n.991C>A | ||
NM_000322.5:c.286C>A MANE Select | NP_000313.2:p.Pro96Thr |